rs10490823

Orientation

minus

Stabilized

minus

Make rs10490823(A;A)

Make rs10490823(A;G)

Make rs10490823(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

41082244

is a	snp
is	mentioned by
dbSNP	rs10490823
dbSNP (classic)	rs10490823
ClinGen	rs10490823
ebi	rs10490823
HLI	rs10490823
Exac	rs10490823
Gnomad	rs10490823
Varsome	rs10490823
LitVar	rs10490823
Map	rs10490823
PheGenI	rs10490823
Biobank	rs10490823
1000 genomes	rs10490823
hgdp	rs10490823
ensembl	rs10490823
geneview	rs10490823
scholar	rs10490823
google	rs10490823
pharmgkb	rs10490823
gwascentral	rs10490823
openSNP	rs10490823
23andMe	rs10490823
SNPshot	rs10490823
SNPdbe	rs10490823
MSV3d	rs10490823
GWAS Ctlg	rs10490823

GMAF

0.3416

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 19079262]
Trait	Bone mineral density (hip)
Title	New sequence variants associated with bone mineral density
Risk Allele	G
P-val	0.000009
Odds Ratio	0.06 [0.03-0.09] SD decrease